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基于自动化质谱的硫酸化糖胺聚糖分析筛选方法。

An automated mass spectrometry-based screening method for analysis of sulfated glycosaminoglycans.

机构信息

Department of Chemistry-BMC, Uppsala University, Box 599, 751 24 Uppsala, Sweden; Science for Life Laboratory, Uppsala University, Box 599, 751 24 Uppsala, Sweden.

Department of Medical Biochemistry and Microbiology, Uppsala University, Box 582, 751 23 Uppsala, Sweden.

出版信息

Biochem Biophys Res Commun. 2014 Jul 18;450(1):598-603. doi: 10.1016/j.bbrc.2014.06.011. Epub 2014 Jun 10.

Abstract

Glycosaminoglycans (GAGs) are linear polysaccharides, consisting of repeated disaccharide units, attached to core proteins in all multicellular organisms. Chondroitin sulfate (CS) and dermatan sulfate (DS) constitute a subgroup of sulfated GAGs for which the degree of sulfation varies between species and tissues. One major goal in GAG characterization is to correlate structure to function. A common approach is to exhaustively degrade the GAG chains and thereafter determine the amount of component disaccharide units. In large-scale studies, there is a need for high-throughput screening methods since existing methods are either very time- or samples consuming. Here, we present a new strategy applying MALDI-TOF MS in positive ion mode for semi-qualitative and quantitative analysis of CS/DS derived disaccharide units. Only a few picomoles of sample are required per analysis and 10 samples can be analyzed in 25 min, which makes this approach an attractive alternative to many established assay methods. The total CS/DS concentration in 19 samples derived from Caenorhabditis elegans and mammalian tissues and cells was determined. The obtained results were well in accordance with concentrations determined by a standard liquid chromatography-based method, demonstrating the applicability of the method for samples from various biological matrices containing CS/DS of different sulfation degrees.

摘要

糖胺聚糖(GAGs)是线性多糖,由重复的二糖单元组成,连接在所有多细胞生物的核心蛋白上。软骨素硫酸盐(CS)和皮肤素硫酸盐(DS)构成了硫酸化 GAGs 的一个亚组,其硫酸化程度在物种和组织之间有所不同。GAG 特性分析的一个主要目标是将结构与功能相关联。一种常见的方法是彻底降解 GAG 链,然后确定成分二糖单元的数量。在大规模研究中,需要高通量筛选方法,因为现有的方法要么非常耗时,要么消耗大量样本。在这里,我们提出了一种新的策略,即在正离子模式下应用 MALDI-TOF MS 对半定量和定量分析 CS/DS 衍生的二糖单元。每个分析只需几个皮摩尔的样品,并且可以在 25 分钟内分析 10 个样品,这使得这种方法成为许多已建立的分析方法的有吸引力的替代方法。从秀丽隐杆线虫和哺乳动物组织和细胞中提取的 19 个样本中的总 CS/DS 浓度被确定。得到的结果与基于标准液相色谱法确定的浓度非常一致,证明了该方法适用于含有不同硫酸化程度 CS/DS 的各种生物基质样本。

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